A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235534



Internal ID20802574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58673201..58679100hg38UCSC Ensembl
chr8:59585760..59591659hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235534
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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